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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10480 | Bay 41-4109 (less active enantiomer) | HBV | |
Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM). | |||
T11129L | Duvelisib (R enantiomer) hydrochloride | IPI-145 R enantiomer HCl,Duvelisib (R enantiomer) hydrochloride(1261590-48-0 Free base),INK1197 R enantiomer HCl | PI3K |
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib. | |||
T12831 | SAR405 R enantiomer | Others | |
SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. | |||
T20191 | (-)-Camphoric acid | L-Camphoric acid,Camphoric acid, (-)- | GluR |
(-)-Camphoric acid (L-Camphoric acid) is a less active enantiomer of Camphoric acid which induces GluR expression. | |||
T22450 | Tyrphostin B44, (+) enantiomer | EGFR | |
Tyrphostin B44, (+) enantiomer is an inhibitor of epidermal growth factor receptor (EGFR) kinase with IC50 of 0.86 μM and has less active than the (-) enantiomer. | |||
T12814 | (S)-Tenofovir | (S)-PMPA,(S)-GS 1278,(S)-TDF | Others |
(S)-Tenofovir ((S)-PMPA) is the less active S-enantiomer of Tenofovir which is a nucleotide reverse transcriptase inhibitor. | |||
T10376 | ARS-1630 | Ras | |
ARS-1630 is a mutant K-ras G12C inhibitor. It is a less active enantiomer of ARS-1620. | |||
T13140 | Umbralisib R-enantiomer | TGR-1202 R-enantiomer,RP5264 R-enantiomer | PI3K |
Umbralisib R-enantiomer (RP5264 R-enantiomer) is a delta inhibitor of PI3K and a less active enantiomer of TGR-1202. The IC50 of Umbralisib R-enantiomers against δPI3 kinase is at least 20 times lower than that of the in... | |||
T20898 | (R)-Propranolol hydrochloride | Dexpropranolol hydrochloride,(R)-(+)-Propranolol | Adrenergic Receptor |
(R)-Propranolol hydrochloride (Dexpropranolol hydrochloride) is the less active enantiomer of the anti-adrenoceptor (β-adrenoceptor) antagonist propranolol. Propranolol is a nonselective β-adrenergic receptor (βAR) antag... | |||
TN1448 | (-)-Bornyl acetate | L-(-)-Bornyl acetate,Bornyl acetate | p38 MAPK , NF-κB , JNK , Antifungal |
(-)-Bornyl acetate (L-(-)-Bornyl acetate) is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate isolates from hyssop oil and possesses antifungal activity. (-)-Bornyl acetate shows highly active whitening... | |||
T13438 | (R,S)-Ivosidenib | (R,S)-AG-120 | Opioid Receptor |
(R,S)-Ivosidenib is the less active enantiomer of Ivosidenib . | |||
T13450 | (S)-GNE-140 | Others | |
(S)-GNE-140 is the less active enantiomer of GNE-140. | |||
T11156 | Nazartinib S-enantiomer | EGF816 (S-enantiomer) | Others |
Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib. | |||
T10856 | Cobimetinib (R-enantiomer) | XL-518 R-enantiomer,Cobimetinib R-enantiomer,GDC-0973 R-enantiomer | Others |
Cobimetinib R-enantiomer is the less active R-enantiomer of Cobimetinib which is a selective MEK inhibitor. | |||
T13426L | (3S,4S)-Tofacitinib | Others | |
(3S,4S)-Tofacitinib, a less active enantiomer of tofacitinib, is a Janus kinases inhibitor. | |||
T26371 | (2S,3R)-LP99 | ||
(2S,3R)-LP99 is a less active enantiomer of LP99. | |||
T10564 | (8R,9S)-Talazoparib | (8R,9S)-BMN-673 | Others |
(8R,9S)-Talazoparib is Talazoparib enantiomer , less active than Talazoparib on the inhibition of PARP1 (IC50: 144 nM). | |||
T12636 | (R)-(+)-Anatabine | Others | |
(R)-(+)-Anatabine is an less active R-enantiomer of Anatabine. Anatabine is a potent agonist of α4β2 nAChR. | |||
T11335 | Fulvestrant (S enantiomer) | ZM 182780 S enantiomer,ICI 182780 S enantiomer,Fulvestrant S enantiomer,ZD 9238 S enantiomer | Others |
Fulvestrant S enantiomer is the less active S enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM. | |||
T12635 | (R)-Plevitrexed | (R)-ZD 9331,(R)-BGC9331 | Others |
(R)-Plevitrexed is a less active enantiomer of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS). |